CN113067095A - Three-dimensional porous elastic diaphragm and preparation and application thereof - Google Patents
Three-dimensional porous elastic diaphragm and preparation and application thereof Download PDFInfo
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- CN113067095A CN113067095A CN201911287579.3A CN201911287579A CN113067095A CN 113067095 A CN113067095 A CN 113067095A CN 201911287579 A CN201911287579 A CN 201911287579A CN 113067095 A CN113067095 A CN 113067095A
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/054—Accumulators with insertion or intercalation of metals other than lithium, e.g. with magnesium or aluminium
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/05—Accumulators with non-aqueous electrolyte
- H01M10/056—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
- H01M10/0564—Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of organic materials only
- H01M10/0565—Polymeric materials, e.g. gel-type or solid-type
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M2220/00—Batteries for particular applications
- H01M2220/30—Batteries in portable systems, e.g. mobile phone, laptop
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
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Abstract
Compared with the currently used gel electrolyte elastic diaphragm, the three-dimensional porous solid diaphragm has better mechanical property and higher elasticity, cannot be damaged after repeated expansion and contraction, and prevents internal short circuit; compared with gel-state electrolyte, the liquid electrolyte filled in the film has higher ionic conductivity, and the rate performance of the assembled battery is more excellent; meanwhile, the method has the advantages of simple preparation process and low energy consumption, and is suitable for large-scale production.
Description
Technical Field
The invention belongs to the field of elastic battery diaphragms, and discloses a three-dimensional porous elastic diaphragm and a preparation method and application thereof.
Background
Flexible electronic devices are gaining increasing attention for their potential use in wearable devices, implantable medical devices, electronic skin devices, and the like. To meet the requirements of reliable elastic electronics, it is important to develop deformable energy storage devices. At present, some researches have been successfully carried out to prepare deformable power supply devices, such as elastic lithium ion batteries, elastic sodium ion batteries, elastic supercapacitors, elastic silver-zinc batteries, and the like. However, the current work mainly focuses on the preparation of the elastic electrode and the design of the elastic structure, and the research on the diaphragm is very little. While the separator serves as a critical component of the battery, the development of the separator is crucial to the research of elastic devices.
The separator used in the present elastic device is basically a gel electrolyte due to controllability and deformability of the gel electrolyte. But the ionic conductivity of the gel electrolyte is low compared to a liquid electrolyte, resulting in poor rate performance of the assembled battery. Meanwhile, the gel electrolyte has poor mechanical properties and is easy to crack in a repeated stretching process, so that the contact between a positive electrode and a negative electrode is caused, and internal short circuit is caused. In order to realize safe and stable output of elastic power supply equipment in the repeated stretching process, the development of a solid elastic diaphragm which is not easy to break is urgently needed.
Disclosure of Invention
The invention prepares a three-dimensional porous solid elastic material.
The adopted specific technical scheme is as follows: a method of making a three-dimensional porous elastic membrane, the elastic membrane being made by the steps of:
1) adding one or more than two elastic macromolecules into a solvent, and fully stirring for 0.5-48 h at the temperature of 20-100 ℃ to prepare a solution A;
2) pouring the solution A prepared in the step (1) on an aluminum foil or directly on a flat plate, volatilizing the solvent for 0-60 minutes, then soaking the whole in a poor solvent of an elastic macromolecule for 1-300 minutes, and preparing a porous membrane at the temperature of 0-60 ℃;
3) and (3) drying the porous membrane prepared in the step (2) at the temperature of 0-200 ℃ for 1-24 hours to obtain the elastic membrane.
Based on the above technical scheme, preferably, the elastic polymer in step 1) is one or more of styrene butadiene rubber, polyisoprene, polystyrene-polybutadiene-polystyrene block copolymer, ethylene propylene rubber, butadiene acrylonitrile rubber and butadiene rubber.
Based on the technical scheme, preferably, the solvent of the elastic polymer in the step 1) is one or more than two of cyclohexane, toluene, benzene, ethyl acetate, dichloroethane and tetrahydrofuran; wherein the concentration of the elastic polymer in the solution is 2-70 wt%, preferably 5-20 wt%.
Based on the technical scheme, preferably, the poor solvent of the elastic polymer in the step 2) is one or more of methanol, ethanol, n-propanol, n-butanol, water and DMF.
Based on the technical scheme, preferably, the solvent volatilization time in the step 2) is 0-60 minutes, preferably 0-10 minutes, and the time for immersing the resin in the poor solvent is 1-300 minutes, preferably 5-100 minutes.
The invention also provides the three-dimensional porous elastic material prepared by the preparation method, and the tensile breaking point of the three-dimensional elastic material is 600-1400%.
Based on the above technical solution, preferably, the elastic material is in a solid state.
Based on the technical scheme, the elastic material is preferably a three-dimensional porous material, and the pore diameter range is 500nm-10 μm. .
The elastic material is used as a diaphragm in an elastic sodium-ion battery.
Advantageous effects
(1) Compared with the currently used gel electrolyte elastic diaphragm, the three-dimensional porous solid diaphragm prepared by the invention has more excellent elastic performance, can meet higher elastic requirements, and has higher practicability and wider application range.
(2) The three-layer porous elastic diaphragm prepared by the invention is used as a solid diaphragm, has better mechanical property, can not be damaged even after repeated expansion and contraction, can well separate a positive electrode and a negative electrode, prevents internal short circuit, and improves the reliability and the safety of elastic equipment.
(3) Compared with gel-state electrolyte, the three-dimensional porous elastic diaphragm has higher ionic conductivity when being filled with liquid electrolyte in the assembled battery, can ensure the rapid conduction of ions in the diaphragm, and has more excellent rate performance.
(4) The preparation method of the three-dimensional porous elastic diaphragm is simple in process, low in energy consumption and suitable for large-scale production.
Drawings
FIG. 1 is an SEM photograph of example 1.
FIG. 2 is a charge and discharge curve at 100mA/g for example 1 and comparative example 1.
Detailed Description
Example 1
(elastic diaphragm made of styrene-butadiene rubber)
1.0g of styrene-butadiene rubber (elastic polymer) was weighed into 9.0g of toluene, and stirred for several hours until completely dissolved to form a 10% polymer solution. And flatly paving the mixed solution on a glass plate, setting the paving thickness to be 200 mu m, then quickly soaking the glass plate in 5L of ethanol for 30 minutes, curing and drying the glass plate at 50 ℃ for 12 hours to obtain the final styrene-butadiene rubber elastic diaphragm. Mixing Na3V2(PO4)3The @ C electrode is used as a working electrode, the metal sodium sheet is used as a negative electrode, the prepared elastic diaphragm is used as a diaphragm, the solute is 1MNaClO4, the solvent EC (ethylene carbonate) and PC (propylene carbonate) mixture (the mass ratio is 1:1), the additive is FEC (forward osmosis) with the mass fraction of 5% and is used as electrolyte, and the sodium-ion battery is assembled by sequentially stacking and compressing a CR2016 button shell according to the sequence of the negative electrode shell, the negative electrode, the electrolyte, the diaphragm, the electrolyte, the positive electrode and the positive electrode shell.
Example 2
(preparation of an elastic Membrane from Polyisoprene)
1.0g of polyisoprene (elastomeric polymer) was weighed into 9.0g of toluene and stirred for several hours until completely dissolved to form a 10% polymer solution. The mixed solution was spread on a glass plate with a film thickness set to 200 μm, then rapidly immersed in 5L of ethanol for 30 minutes, cured, and dried at 50 ℃ for 12 hours to obtain a final polyisoprene elastic membrane. The cell assembly was the same as in example 1.
Example 3
(preparation of an elastic diaphragm from a polystyrene-polybutadiene-polystyrene Block copolymer)
1.0g of polystyrene-polybutadiene-polystyrene block copolymer (elastomeric polymer) was weighed into 9.0g of toluene and stirred for several hours until completely dissolved to form a 10% polymer solution. The mixed solution was spread on a glass plate with a film thickness set to 200 μm, then rapidly immersed in 5L of ethanol for 30 minutes, cured, and dried at 50 ℃ for 12 hours to obtain a final polystyrene-polybutadiene-polystyrene block copolymer elastic membrane.
The cell assembly was the same as in example 1.
Example 4
(ethylene propylene rubber preparation of elastic diaphragm)
1.0g of ethylene-propylene rubber (elastomeric polymer) was weighed into 9.0g of toluene and stirred for several hours until completely dissolved to form a 10% polymer solution. And flatly paving the mixed solution on a glass plate, setting the paving thickness to be 200 mu m, then quickly soaking the glass plate in 5L of ethanol for 30 minutes, curing and drying the glass plate at 50 ℃ for 12 hours to obtain the final ethylene propylene rubber elastic diaphragm. The cell assembly was the same as in example 1.
Example 5
(preparation of an elastic diaphragm from butadiene rubber)
1.0g of butadiene rubber (elastomeric polymer) was weighed into 9.0g of toluene and stirred for several hours until completely dissolved to form a 10% polymer solution. The mixed solution was spread on a glass plate with a film thickness set to 200 μm, then rapidly immersed in 5L of ethanol for 30 minutes, cured, and dried at 50 ℃ for 12 hours to obtain a final cis-butadiene rubber elastic membrane. The cell assembly was the same as in example 1.
Comparative example 1
(gel electrolyte elastic diaphragm)
Mixing dichloromethane and acetone according to the mass ratio of 40:1 to obtain a mixed solution, adding 0.35g of polyethylene oxide, 0.35g of succinonitrile and 0.30g of sodium bistrifluoromethylsulfonate into the mixed solution, and stirring to obtain uniform gel. The gel was then laid on a glass plate with the thickness set to 200 μm, and dried for 30 minutes to obtain a gel electrolyte elastic separator. The Na3V2(PO4)3@ C electrode is used as a working electrode, a metal sodium sheet is used as a negative electrode, the prepared gel electrolyte diaphragm is used as a diaphragm, and the sodium ion battery is assembled by sequentially stacking and compressing a CR2016 button type shell according to the sequence of a negative electrode shell, a negative electrode, the diaphragm, a positive electrode and a positive electrode shell.
Comparative example 2
(preparation of elastic diaphragm by PBI Membrane preparation Process)
An attempt was made to dissolve 1.0g of styrene-butadiene rubber in DMF (N, N-dimethylformamide), and styrene-butadiene rubber was not soluble in DMF because of the large difference in polarity between styrene-butadiene rubber and DMF. It can be seen that the conventional electrode separator preparation process cannot be used for preparing an elastic separator.
As can be seen from fig. 1, the elastic separator of example 1 has micro-scale or more large pores on both the front and back surfaces thereof, and the pores extend into the interior of the separator to form a continuous channel. The coherent macropores can ensure the infiltration of liquid electrolyte, thereby forming an ion transmission channel in the diaphragm and ensuring the rapid transmission of ions in the diaphragm.
As can be seen from FIG. 2, example 1 exhibited 113mAh g at a current of 100mA/g-1Specific capacity of (2), whereas the comparative example shows only 87mAh g-1The specific capacity of (A). This is because the liquid electrolyte used in example 1 has a faster sodium ion transport rate, is more favorable for capacity exertion of the positive electrode material, and thus exhibits a higher specific capacity, as compared to the gel electrolyte of the comparative example. Also, example 1 shows excellent mechanical properties and stability without breakage after a stretching cycle at 200% strain, compared to the breakage easiness of the gel electrolyte.
Moreover, example 1 also exhibited extremely high elasticity. The tensile breaking point of example 1 is 850%, meaning that the elastic membrane can achieve a stretch ratio of 850%. Example 1 in the case of a 200% expansion and contraction ratio, the battery still exhibited 108mAh g when the electrode was assembled-1The specific capacity of the composite material is excellent in elasticity and electrochemical performance.
Claims (9)
1. A preparation method of a three-dimensional porous elastic material is characterized by comprising the following steps: the method comprises the following steps:
1) adding an elastic high polymer material into a solvent, and fully stirring for 0.5-48 hours at the temperature of 20-100 ℃ to prepare a solution A;
2) pouring the solution A on an aluminum foil or directly on a flat plate, volatilizing the solvent for 0-60 minutes, and then soaking the whole body in a poor solvent of an elastic macromolecule at 0-60 ℃ for 1-300 minutes to obtain a porous membrane;
3) and (3) drying the porous membrane prepared in the step (2) at the temperature of 0-200 ℃ for 1-24 hours to prepare the three-dimensional porous elastic material.
2. The method of claim 1, wherein: in the step 1), the elastic high polymer material is at least one of styrene-butadiene rubber, polyisoprene, polystyrene-polybutadiene-polystyrene block copolymer, ethylene propylene rubber, butadiene-acrylonitrile rubber and butadiene rubber.
3. The method of claim 1, wherein: the solvent in the step 1) is at least one of cyclohexane, toluene, benzene, ethyl acetate, dichloroethane and tetrahydrofuran; the concentration of the elastic polymer material in the solution A is 2-70 wt%, preferably 5-20 wt%.
4. The method of claim 1, wherein: the poor solvent of the elastic polymer in the step 2) is at least one of methanol, ethanol, n-propanol, n-butanol, water and DMF.
5. The method of claim 1, wherein: the solvent in the step 2) is volatilized for 0-10 minutes, and the resin is immersed in the poor solvent for 5-100 minutes.
6. A three-dimensional porous elastic material obtainable by the process according to any one of claims 1 to 5, characterized in that said three-dimensional elastic material has a tensile breaking point of between 600% and 1400%.
7. The three-dimensional porous elastomeric material according to claim 6, wherein said elastomeric material is in a solid state.
8. The three-dimensional porous elastic material according to claim 6, wherein said elastic material is a three-dimensional porous material having a pore size in the range of 500nm to 10 μm.
9. Use of the elastic separator membrane according to claims 6-8, said three-dimensional porous elastic material being used as a separator membrane in elastic sodium-ion batteries.
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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CN102751459A (en) * | 2011-04-22 | 2012-10-24 | 北京东皋膜技术有限公司 | Nano microporous diaphragm made of post-crosslinked rubber and polyolefin composite, and manufacturing method thereof |
CN103022530A (en) * | 2012-12-14 | 2013-04-03 | 辽宁师范大学 | Porous membrane and preparation method as well as application thereof in fuel battery |
CN103078076A (en) * | 2013-01-11 | 2013-05-01 | 宁波晶一新材料科技有限公司 | Composite diaphragm and lithium ion battery employing same |
CN108134107A (en) * | 2016-12-01 | 2018-06-08 | 中国科学院大连化学物理研究所 | A kind of perforated membrane is in the application of Alkaline Zinc iron liquid galvanic battery |
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102751459A (en) * | 2011-04-22 | 2012-10-24 | 北京东皋膜技术有限公司 | Nano microporous diaphragm made of post-crosslinked rubber and polyolefin composite, and manufacturing method thereof |
CN103022530A (en) * | 2012-12-14 | 2013-04-03 | 辽宁师范大学 | Porous membrane and preparation method as well as application thereof in fuel battery |
CN103078076A (en) * | 2013-01-11 | 2013-05-01 | 宁波晶一新材料科技有限公司 | Composite diaphragm and lithium ion battery employing same |
CN108134107A (en) * | 2016-12-01 | 2018-06-08 | 中国科学院大连化学物理研究所 | A kind of perforated membrane is in the application of Alkaline Zinc iron liquid galvanic battery |
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